SPATC1L variants associated with age-related and hereditary hearing loss
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https://www.omicsdi.org/dataset/ega/EGAS00001003047
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资源简介：
Next-Generation Sequencing techniques (i.e, targeted re-sequencing and whole exome sequencing) have been employed for the study of two Italian patients affected by age-related hearing loss and of an Italian family affected by hereditary hearing loss. Data analysis led to the identification of three variants in SPATC1L, associated with the clinical phenotype.EGA study EGAS00001003047
创建时间：
2018-06-18
